Tate Genshu, Hirayama-Ohashi Yoshiko, Kishimoto Koji, Mitsuya Toshiyuki
Department of Surgical Pathology, Showa University Fujigaoka Hospital, Fujigaoka 1-30, Aoba-ku, Yokohama 227-8501, Japan.
Cancer Genet Cytogenet. 2007 Jan 15;172(2):151-3. doi: 10.1016/j.cancergencyto.2006.08.005.
B lymphocyte-induced maturation protein 1 (BLIMP1)/PR domain containing 1 with zinc finger domain (PRDM1) is a transcriptional repressor with a SET domain and Kruppel-type zinc fingers. BLIMP1/PRDM1 is expressed in a subset of germinal center B cells and in all plasma cells, and it is required for terminal B-cell differentiation. Mutations of the BLIMP1 gene have been reported in patients with diffuse large B-cell lymphoma. Here, we describe novel mutations in the BLIMP1 gene in 2 of 15 (13%) cases of B-cell lymphoma (two cases of primary effusion lymphoma and 13 cases of diffuse large B-cell lymphoma). A tandem 10-base pair duplication (5'-GCTGAGTTTG-3') was found in exon 2 of the BLIMP1 gene in primary effusion B-cell lymphoma. We also found in diffuse large B-cell lymphoma a single base substitution in exon 6 (1747C-->T) that results in a somatic nonsense mutation (Q583X). These findings indicate that mutational analysis of the BLIMP1 gene may be useful for characterizing the molecular basis of B-cell lymphoma.
B淋巴细胞诱导成熟蛋白1(BLIMP1)/含锌指结构域的PR结构域蛋白1(PRDM1)是一种具有SET结构域和克鲁ppel型锌指的转录抑制因子。BLIMP1/PRDM1在生发中心B细胞亚群和所有浆细胞中表达,是B细胞终末分化所必需的。在弥漫性大B细胞淋巴瘤患者中已报道了BLIMP1基因的突变。在此,我们描述了15例B细胞淋巴瘤(2例原发性渗出性淋巴瘤和13例弥漫性大B细胞淋巴瘤)中有2例(13%)的BLIMP1基因存在新突变。在原发性渗出性B细胞淋巴瘤的BLIMP1基因第2外显子中发现了一个10碱基对的串联重复(5'-GCTGAGTTTG-3')。我们还在弥漫性大B细胞淋巴瘤中发现第6外显子有一个单碱基替换(1747C→T),导致一个体细胞无义突变(Q583X)。这些发现表明,BLIMP1基因的突变分析可能有助于表征B细胞淋巴瘤的分子基础。